Wound dressings and methods of use with integrated negative pressure source having a fluid ingress inhibition component

ABSTRACT

Disclosed embodiments relate to apparatuses and methods for wound treatment. In some embodiments, a negative pressure source is incorporated into a wound dressing apparatus so that the wound dressing and the negative pressure source are part of an integral or integrated wound dressing structure that applies the wound dressing and the negative pressure source simultaneously to a patient&#39;s wound. The negative pressure source and/or electronic components may be positioned between a wound contact layer and a cover layer of the wound dressing. A component may be used to prevent wound exudate from contacting the inlet of the negative pressure source.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation application of U.S. application Ser. No. 16/096,266, filed Oct. 24, 2018, which is a U.S. national stage application of International Patent Application No. PCT/EP2017/059883, filed Apr. 26, 2017, which claims priority to U.S. Provisional Application No. 62/327,676, filed Apr. 26, 2016.

BACKGROUND Technical Field

Embodiments described herein relate to apparatuses, systems, and methods for the treatment of wounds, for example using dressings in combination with negative pressure wound therapy.

Description of the Related Art

The treatment of open or chronic wounds that are too large to spontaneously close or otherwise fail to heal by means of applying negative pressure to the site of the wound is well known in the art. Negative pressure wound therapy (NPWT) systems currently known in the art commonly involve placing a cover that is impermeable or semi-permeable to fluids over the wound, using various means to seal the cover to the tissue of the patient surrounding the wound, and connecting a source of negative pressure (such as a vacuum pump) to the cover in a manner so that negative pressure is created and maintained under the cover. It is believed that such negative pressures promote wound healing by facilitating the formation of granulation tissue at the wound site and assisting the body's normal inflammatory process while simultaneously removing excess fluid, which may contain adverse cytokines and/or bacteria. However, further improvements in NPWT are needed to fully realize the benefits of treatment.

Many different types of wound dressings are known for aiding in NPWT systems. These different types of wound dressings include many different types of materials and layers, for example, gauze, pads, foam pads or multi-layer wound dressings. One example of a multi-layer wound dressing is the PICO dressing, available from Smith & Nephew, which includes a superabsorbent layer beneath a backing layer to provide a canister-less system for treating a wound with NPWT. The wound dressing may be sealed to a suction port providing connection to a length of tubing, which may be used to pump fluid out of the dressing and/or to transmit negative pressure from a pump to the wound dressing.

Prior art dressings for use in negative pressure such as those described above have included a negative pressure source located in a remote location from the wound dressing. Negative pressure sources located remote from the wound dressing have to be held by or attached to the user or other pump support mechanism. Additionally, a tubing or connector is required to connect the remote negative pressure source to the wound dressing. The remote pump and tubing can be cumbersome and difficult to hide in or attach to patient clothing. Depending on the location of the wound dressing, it can be difficult to comfortably and conveniently position the remote pump and tubing. When used, wound exudate may soak into the dressing, and the moisture from the wound has made it difficult to incorporate electronic components into the dressing.

SUMMARY

Embodiments of the present disclosure relate to apparatuses and methods for wound treatment. Some of the wound treatment apparatuses described herein comprise a negative pressure source or a pump system for providing negative pressure to a wound. Wound treatment apparatuses may also comprise wound dressings that may be used in combination with the negative pressure sources and pump assemblies described herein. In some embodiments, a negative pressure source is incorporated into a wound dressing apparatus so that the wound dressing and the negative pressure source are part of an integral or integrated wound dressing structure that applies the wound dressing and the negative pressure source simultaneously to a patient's wound. The negative pressure source and/or electronic components may be positioned between a wound contact layer and a cover layer of the wound dressing. A component may be used to prevent wound exudate from contacting the inlet of the negative pressure source. These and other embodiments as described herein are directed to overcoming particular challenges involved with incorporating a negative pressure source and/or electronic components into a wound dressing.

In some aspects, a wound dressing apparatus comprises a wound dressing configured to be positioned over a wound site, the wound dressing comprising a wound contact layer configured to be positioned in contact with a wound, a first area and a second area positioned adjacent to the first area, wherein the first area comprises an absorbent material and the second area is configured to receive a negative pressure source, and a cover layer configured to cover and form a seal over the wound contact layer, the first area, and the second area, a negative pressure source disposed on or positioned within the second area of the wound dressing, the negative pressure source comprising an inlet and an outlet and being operable to apply negative pressure to the wound site, and a component in fluid communication with the inlet, the component defining a plurality of flow paths between an interior of the wound dressing and the inlet such that occlusion of the inlet is inhibited, and wherein the component is in fluid communication with the absorbent material and configured to inhibit flow of wound exudate from the wound site into the inlet.

The apparatus of the preceding paragraph may also include any combination of the following features described in this paragraph, among others described herein. Each of the features described in the following paragraphs may also be part of another embodiment that does not necessarily include all of the features of the previous paragraph. The component can comprise a hydrophobic material configured to repel wound exudate. The component can comprise a material having a pore size configured to resist ingress of wound exudate due to capillary action. The component can comprise one or more porous polymer molded components. The polymer comprising the one or more porous polymer molded components can be hydrophobic and can have a pore size in the range of approximately 20 microns to approximately 40 microns. The pore size can be approximately 30 microns. The polymer comprising the one or more porous polymer molded components can be hydrophobic and can have a pore size in the range of approximately 5 microns to approximately 40 microns. The pore size can be approximately 10 microns.

The polymer can be POREX® or PORVAIR®. The polymer can be one of hydrophobic polyethylene or hydrophobic polypropylene. Each of the one or more porous polymer molded components can be configured to increase the contact area between the pump inlet and the interior of the wound dressing. The one or more porous polymer components have a three-dimensional shape. For example, the one or more porous polymer components can be crescent-shaped, thimble-shaped, or cuboid or generally cuboid shaped. The one or more porous polymer components can also have curved or beveled corners and/or edges. The one or more porous polymer components can be configured to attach to at least one of the inlet and an end of a tubular extension in fluid communication with the inlet and the interior of the wound dressing.

The component can comprise one or more micro porous membranes attached to the inlet. The wound dressing apparatus can comprise a spacer material disposed within the membrane, the spacer material configured to inhibit the membrane from collapsing. The micro porous membrane can comprise Versapore having a 0.2 micron pore size (Pall). The component can comprise one or more lengths of fine bore tubing defining a plurality of holes along their lengths. The one or more lengths of fine bore tubing can form one or more loops between the inlet and the wound dressing. The one or more lengths of fine bore tubing can extend from the inlet to one or more different points in the wound dressing. The negative pressure source can be a micro pump. The wound dressing apparatus can comprise a controller configured to control the operation of the micro pump to apply negative pressure to the wound site. The absorbent material can be configured to absorb wound exudate. The component can be attached to the inlet. The component can be fitted to the inlet.

In one embodiment, a wound dressing apparatus comprises a wound dressing configured to be positioned over a wound site, a negative pressure source disposed on or positioned within the wound dressing, the negative pressure source comprising an inlet and an outlet and being operable to apply negative pressure to the wound site, and a porous polymer component fitted to the inlet of the negative pressure source and in fluid communication with the inlet, the porous polymer component comprising a three-dimensional body defining a plurality of flow paths between an interior of the wound dressing and the inlet such that occlusion of the inlet is inhibited.

The porous polymer component can comprise a hydrophobic material configured to repel wound exudate. The porous polymer component can have a pore size in the range of approximately 20 microns to approximately 40 microns. The pore size can be approximately 30 microns. The porous polymer component can have a pore size in the range of approximately 5 microns to approximately 40 microns. The pore size can be approximately 10 microns. The polymer can be PORVAIR Vyon®. The porous polymer component can be crescent-shaped, thimble-shaped, or cuboid or generally cuboid shaped. The porous polymer component can also have curved or beveled corners and/or edges.

Any of the features, components, or details of any of the arrangements or embodiments disclosed in this application, including without limitation any of the pump embodiments and any of the negative pressure wound therapy embodiments disclosed below, are interchangeably combinable with any other features, components, or details of any of the arrangements or embodiments disclosed herein to form new arrangements and embodiments.

BRIEF DESCRIPTION OF THE DRAWINGS

Embodiments of the present disclosure will now be described hereinafter, by way of example only, with reference to the accompanying drawings in which:

FIG. 1 illustrates an embodiment of a wound treatment apparatus including a wound dressing in combination with a pump;

FIG. 2 illustrates an embodiment of a source of negative pressure and battery included within an integrated dressing;

FIGS. 3A-3B illustrate an embodiment of a wound dressing incorporating the source of negative pressure and/or other electronic components within the wound dressing;

FIG. 3C is a side cross-sectional view of a wound dressing system with one or more embedded electronic components;

FIG. 4A illustrates an embodiment of a component directly coupled to the pump inlet;

FIGS. 4B and 4C illustrate an embodiment of components indirectly coupled to the pump inlet via an intermediate tubular member;

FIGS. 5A-5C illustrate cross-sectional views of the corresponding components shown in FIGS. 4A-4C;

FIGS. 6A and 6B illustrate a fluid ingress inhibition system similar to the system;

FIG. 7A illustrates the top view of an electronics unit including a pump and a component directly coupled to the pump inlet;

FIG. 7B illustrates a bottom or wound facing surface of an electronics unit including a pump and a component directly coupled to the pump inlet;

FIG. 8 illustrates an embodiment of the layers of a wound dressing incorporating the source of negative pressure and/or other electronic components within the wound dressing; and

FIGS. 9A and 9B illustrate an embodiment of a component with a port for coupling to the pump inlet.

DETAILED DESCRIPTION

Embodiments disclosed herein relate to apparatuses and methods of treating a wound with reduced pressure, including a source of negative pressure and wound dressing components and apparatuses. The apparatuses and components including the wound overlay and packing materials, if any, are sometimes collectively referred to herein as dressings.

It will be appreciated that throughout this specification reference is made to a wound. It is to be understood that the term wound is to be broadly construed and encompasses open and closed wounds in which skin is torn, cut or punctured or where trauma causes a contusion, or any other superficial or other conditions or imperfections on the skin of a patient or otherwise that benefit from reduced pressure treatment. A wound is thus broadly defined as any damaged region of tissue where fluid may or may not be produced. Examples of such wounds include, but are not limited to, abdominal wounds or other large or incisional wounds, either as a result of surgery, trauma, sterniotomies, fasciotomies, or other conditions, dehisced wounds, acute wounds, chronic wounds, subacute and dehisced wounds, traumatic wounds, flaps and skin grafts, lacerations, abrasions, contusions, bums, diabetic ulcers, pressure ulcers, stoma, surgical wounds, trauma and venous ulcers or the like.

It will be understood that embodiments of the present disclosure are generally applicable to use in topical negative pressure (“TNP”) therapy systems. Briefly, negative pressure wound therapy assists in the closure and healing of many forms of “hard to heal” wounds by reducing tissue oedema; encouraging blood flow and granular tissue formation; removing excess exudate and may reduce bacterial load (and thus infection risk). In addition, the therapy allows for less disturbance of a wound leading to more rapid healing. TNP therapy systems may also assist on the healing of surgically closed wounds by removing fluid and by helping to stabilize the tissue in the apposed position of closure. A further beneficial use of TNP therapy can be found in grafts and flaps where removal of excess fluid is important and close proximity of the graft to tissue is required in order to ensure tissue viability.

As is used herein, reduced or negative pressure levels, such as −X mmHg, represent pressure levels relative to normal ambient atmospheric pressure, which can correspond to 760 mmHg (or 1 atm, 29.93 inHg, 101.325 kPa, 14.696 psi, etc.). Accordingly, a negative pressure value of −X mmHg reflects absolute pressure that is X mmHg below 760 mmHg or, in other words, an absolute pressure of (760−X) mmHg. In addition, negative pressure that is “less” or “smaller” than X mmHg corresponds to pressure that is closer to atmospheric pressure (e.g., −40 mmHg is less than −60 mmHg). Negative pressure that is “more” or “greater” than −X mmHg corresponds to pressure that is further from atmospheric pressure (e.g., −80 mmHg is more than −60 mmHg). In some embodiments, local ambient atmospheric pressure is used as a reference point, and such local atmospheric pressure may not necessarily be, for example, 760 mmHg.

The negative pressure range for some embodiments of the present disclosure can be approximately −80 mmHg, or between about −20 mmHg and −200 mmHg. Note that these pressures are relative to normal ambient atmospheric pressure, which can be 760 mmHg. Thus, −200 mmHg would be about 560 mmHg in practical terms. In some embodiments, the pressure range can be between about −40 mmHg and −150 mmHg. Alternatively, a pressure range of up to −75 mmHg, up to −80 mmHg or over −80 mmHg can be used. Also, in other embodiments, a pressure range of below −75 mmHg can be used. Alternatively, a pressure range of over approximately −100 mmHg, or even −150 mmHg, can be supplied by the negative pressure apparatus.

In some embodiments of wound closure devices described herein, increased wound contraction can lead to increased tissue expansion in the surrounding wound tissue. This effect may be increased by varying the force applied to the tissue, for example by varying the negative pressure applied to the wound over time, possibly in conjunction with increased tensile forces applied to the wound via embodiments of the wound closure devices. In some embodiments, negative pressure may be varied over time for example using a sinusoidal wave, square wave, and/or in synchronization with one or more patient physiological indices (e.g., heartbeat). Examples of such applications where additional disclosure relating to the preceding may be found include U.S. Pat. No. 8,235,955, titled “Wound treatment apparatus and method,” issued on Aug. 7, 2012; and U.S. Pat. No. 7,753,894, titled “Wound cleansing apparatus with stress,” issued Jul. 13, 2010. The disclosures of both of these patents are hereby incorporated by reference in their entirety.

International Application PCT/GB2012/000587, titled “WOUND DRESSING AND METHOD OF TREATMENT” and filed on Jul. 12, 2012, and published as WO 2013/007973 A2 on Jan. 17, 2013, is an application, hereby incorporated and considered to be part of this specification, that is directed to embodiments, methods of manufacture, and wound dressing components and wound treatment apparatuses that may be used in combination or in addition to the embodiments described herein. Additionally, embodiments of the wound dressings, wound treatment apparatuses and methods described herein may also be used in combination or in addition to those described in U.S. Provisional Application No. 61/650,904, filed May 23, 2012, titled “APPARATUSES AND METHODS FOR NEGATIVE PRESSURE WOUND THERAPY,” International Application No. PCT/IB2013/001469, filed May 22, 2013, titled “APPARATUSES AND METHODS FOR NEGATIVE PRESSURE WOUND THERAPY,” and published as WO 2013/175306 on Nov. 28, 2013, U.S. patent application Ser. No. 14/418,874, filed Jan. 30, 2015, published as U.S. Publication No. 2015/0216733, published Aug. 6, 2015, titled “WOUND DRESSING AND METHOD OF TREATMENT,” U.S. patent application Ser. No. 14/418,908, filed Jan. 30, 2015, published as U.S. Publication No. 2015/0190286, published Jul. 9, 2015, titled “WOUND DRESSING AND METHOD OF TREATMENT,” U.S. patent application Ser. No. 14/658,068, filed Mar. 13, 2015, U.S. Application No. 2015/0182677, published Jul. 2, 2015, titled “WOUND DRESSING AND METHOD OF TREATMENT,” the disclosures of which are hereby incorporated by reference in their entireties. Embodiments of the wound dressings, wound treatment apparatuses and methods described herein may also be used in combination or in addition to those described in U.S. patent application Ser. No. 13/092,042, filed Apr. 21 2011, published as US2011/0282309, titled “WOUND DRESSING AND METHOD OF USE,” and which is hereby incorporated by reference in its entirety, including further details relating to embodiments of wound dressings, the wound dressing components and principles, and the materials used for the wound dressings. Additionally, the present application is related to U.S. Provisional Application No. 62/304,790, filed Mar. 7, 2016, titled “REDUCED PRESSURE APPARATUSES AND METHODS, the subject matter of which is considered to be part of this application and is included in the Appendix below.

FIG. 1 illustrates an embodiment of a TNP wound treatment including a wound dressing 2100 in combination with a pump 2800. As stated above, the wound dressing 2100 can be any wound dressing embodiment disclosed herein or have any combination of features of any number of wound dressing embodiments disclosed herein. Here, the dressing 2100 may be placed over a wound, and a conduit 2220 may then be connected to a port 2150, although in some embodiments the dressing 2100 may be provided with at least a portion of the conduit 2220 preattached to the port 2150. Preferably, the dressing 2100 is provided as a single article with all wound dressing elements (including the port 2150) pre-attached and integrated into a single unit. The wound dressing 2100 may then be connected, via the conduit 2220, to a source of negative pressure such as the pump 2800. The pump 2800 can be miniaturized and portable, although larger conventional pumps may also be used with the dressing 2100. In some embodiments, the pump 2800 may be attached or mounted onto or adjacent the dressing 2100. A connector 2221 may also be provided so as to permit the conduit 2220 leading to the wound dressing 2100 to be disconnected from the pump, which may be useful for example during dressing changes.

In some embodiments, a source of negative pressure (such as a pump) and some or all other components of the TNP system, such as power source(s), sensor(s), connector(s), user interface component(s) (such as button(s), switch(es), speaker(s), screen(s), etc.) and the like, can be integral with the wound dressing. As is illustrated in FIG. 2, the source of negative pressure and battery can be included within the integrated dressing 200. Although FIG. 2 illustrates the source of negative pressure and battery 210 placed on top of the dressing layer 240 (such as an absorbent layer), the source of negative pressure and one or more components can be incorporated into the dressing differently. The source of negative pressure and the one or more components need not all be incorporated into the dressing in the same manner. For example, a pressure sensor can be positioned below (or closer to the wound) the layer 240 while the source of negative pressure can be positioned on top of the layer 240. The integrated dressing 200 illustrated in FIG. 2 includes a cover layer 230 that can secure the dressing to skin surrounding the wound. The cover layer 230 can be formed of substantially fluid impermeable material, such as film (e.g., plastic film). The cover layer can include an adhesive for securing the dressing to the surrounding skin or wound contact layer.

In some embodiments, the dressing can include the power source and other components, such as electronics, on and/or incorporated into the dressing and can utilize a wound contact layer and a first spacer layer within the dressing. The wound contact layer can be in contact with the wound. The wound contact layer can include an adhesive on the patient facing side for securing the dressing to the skin surrounding the wound or on the top side for securing the wound contact layer to a cover layer or other layer of the dressing. In operation, the wound contact layer can provide unidirectional flow so as to facilitate removal of exudate from the wound while blocking or substantially preventing exudate from returning to the wound. The first spacer layer assists in distributing negative pressure over the wound site and facilitating transport of wound exudate and fluids into the wound dressing. Further, an absorbent layer (such as layer 240) for absorbing and retaining exudate aspirated from the wound can be utilized. In some embodiments, the absorbent includes a shaped form of a superabsorber layer with recesses or compartments for the pump, electronics, and accompanying components. These layers can be covered with one or more layers of a film or cover layer (or a first cover layer). The first cover layer can include a filter set that can be positioned within one of the recesses. The filter can align with one of the at least one recesses of the absorbent layer, and the filter can include hydrophobic material to protect the pump and/or other components from liquid exudates. The filter can block fluids while permitting gases to pass through. Optionally, one or more of the pump, electronics, switch and battery can be positioned on top of the first cover layer as illustrated in FIG. 2. Another section of spacer, a second spacer, can be positioned above and/or surrounding the pump. In some embodiments, the second spacer can be smaller than the first spacer used above the wound contact layer. A section of top film or cover layer (or a second cover layer) is positioned over the top of the second spacer with a second filter associated with or positioned within the second cover layer. In some embodiments, the first and second cover layer can be made of the same material. In some embodiments, the first and second cover layers can be made of different material.

In some embodiments, the pump and/or other electronic components can be configured to be positioned adjacent to or next to the absorbent and/or transmission layers so that the pump and/or other electronic components are still part of a single apparatus to be applied to a patient with the pump and/or other electronics positioned away from the wound site. FIGS. 3A-3C illustrates a wound dressing incorporating the source of negative pressure and/or other electronic components within the wound dressing. FIGS. 3A-3C illustrates a wound dressing 1200 with the pump and/or other electronics positioned away from the wound site. The wound dressing can include an electronics area 1261, 1361 and an absorbent area 1260, 1360. The dressing can comprise a wound contact layer 1310 (not shown in FIGS. 3A-3B) and a moisture vapor permeable film or cover layer 1213, 1313 positioned above the contact layer and other layers of the dressing. The wound dressing layers and components of the electronics area as well as the absorbent area can be covered by one continuous cover layer 1213, 1313 as shown in FIGS. 3A-3C.

The dressing can comprise a wound contact layer 1310, a spacer layer 1311, an absorbent layer 1212, 1322, a moisture vapor permeable film or cover layer 1213, 1313 positioned above the wound contact layer, spacer layer, absorbent layer, or other layers of the dressing. The wound contact layer can be configured to be in contact with the wound. The wound contact layer can include an adhesive on the patient facing side for securing the dressing to the surrounding skin or on the top side for securing the wound contact layer to a cover layer or other layer of the dressing. In operation, the wound contact layer can be configured to provide unidirectional flow so as to facilitate removal of exudate from the wound while blocking or substantially preventing exudate from returning to the wound.

The wound contact layer 1310 can be a polyurethane layer or polyethylene layer or other flexible layer which is perforated, for example via a hot pin process, laser ablation process, ultrasound process or in some other way or otherwise made permeable to liquid and gas. The wound contact layer 1310 has a lower surface and an upper surface. The perforations preferably comprise through holes in the wound contact layer 1310 which enable fluid to flow through the layer 1310. The wound contact layer 1310 helps prevent tissue ingrowth into the other material of the wound dressing. Preferably, the perforations are small enough to meet this requirement while still allowing fluid to flow therethrough. For example, perforations formed as slits or holes having a size ranging from 0.025 mm to 1.2 mm are considered small enough to help prevent tissue ingrowth into the wound dressing while allowing wound exudate to flow into the dressing. In some configurations, the wound contact layer 1310 may help maintain the integrity of the entire dressing 1200, 1300 while also creating an air tight seal around the absorbent pad in order to maintain negative pressure at the wound.

Some embodiments of the wound contact layer 1310 may also act as a carrier for an optional lower and upper adhesive layer (not shown). For example, a lower pressure sensitive adhesive may be provided on the lower surface of the wound dressing 1200, 1300 whilst an upper pressure sensitive adhesive layer may be provided on the upper surface of the wound contact layer. The pressure sensitive adhesive, which may be a silicone, hot melt, hydrocolloid or acrylic based adhesive or other such adhesives, may be formed on both sides or optionally on a selected one or none of the sides of the wound contact layer. When a lower pressure sensitive adhesive layer is utilized it may be helpful to adhere the wound dressing 1200, 1300 to the skin around a wound site. In some embodiments, the wound contact layer may comprise perforated polyurethane film. The lower surface of the film may be provided with a silicone pressure sensitive adhesive and the upper surface may be provided with an acrylic pressure sensitive adhesive, which may help the dressing maintain its integrity. In some embodiments, a polyurethane film layer may be provided with an adhesive layer on both its upper surface and lower surface, and all three layers may be perforated together.

A layer 1311 of porous material can be located above the wound contact layer 1310. As used herein, the terms porous material, spacer, and/or transmission layer can be used interchangeably to refer to the layer of material in the dressing configured to distribute negative pressure throughout the wound area. This porous layer, or transmission layer, 1311 allows transmission of fluid including liquid and gas away from a wound site into upper layers of the wound dressing. In particular, the transmission layer 1311 preferably ensures that an open air channel can be maintained to communicate negative pressure over the wound area even when the absorbent layer has absorbed substantial amounts of exudates. The layer 1311 should preferably remain open under the typical pressures that will be applied during negative pressure wound therapy as described above, so that the whole wound site sees an equalized negative pressure. The layer 1311 may be formed of a material having a three-dimensional structure. For example, a knitted or woven spacer fabric (for example Baltex 7970 weft knitted polyester) or a non-woven fabric could be used.

The spacer layer assists in distributing negative pressure over the wound site and facilitating transport of wound exudate and fluids into the wound dressing. In some embodiments, the spacer layer can be formed at least partially from a three-dimensional (3D) fabric.

In some embodiments, the transmission layer 1311 comprises a 3D polyester spacer fabric layer including a top layer (that is to say, a layer distal from the wound-bed in use) which is a 84/144 textured polyester, and a bottom layer (that is to say, a layer which lies proximate to the wound bed in use) which is a 10 denier flat polyester and a third layer formed sandwiched between these two layers which is a region defined by a knitted polyester viscose, cellulose or the like monofilament fiber. Other materials and other linear mass densities of fiber could of course be used.

Whilst reference is made throughout this disclosure to a monofilament fiber it will be appreciated that a multistrand alternative could of course be utilized. The top spacer fabric thus has more filaments in a yarn used to form it than the number of filaments making up the yarn used to form the bottom spacer fabric layer.

This differential between filament counts in the spaced apart layers helps control moisture flow across the transmission layer. Particularly, by having a filament count greater in the top layer, that is to say, the top layer is made from a yarn having more filaments than the yarn used in the bottom layer, liquid tends to be wicked along the top layer more than the bottom layer. In use, this differential tends to draw liquid away from the wound bed and into a central region of the dressing where the absorbent layer 1212,1322 helps lock the liquid away or itself wicks the liquid onwards towards the cover layer 1213, 1313 where it can be transpired.

Preferably, to improve the liquid flow across the transmission layer 1311 (that is to say perpendicular to the channel region formed between the top and bottom spacer layers, the 3D fabric may be treated with a dry cleaning agent (such as, but not limited to, Perchloro Ethylene) to help remove any manufacturing products such as mineral oils, fats or waxes used previously which might interfere with the hydrophilic capabilities of the transmission layer. In some embodiments, an additional manufacturing step can subsequently be carried in which the 3D spacer fabric is washed in a hydrophilic agent (such as, but not limited to, Feran Ice 30 g/l available from the Rudolph Group). This process step helps ensure that the surface tension on the materials is so low that liquid such as water can enter the fabric as soon as it contacts the 3D knit fabric. This also aids in controlling the flow of the liquid insult component of any exudates.

Further, an absorbent layer (such as layer 1212) for absorbing and retaining exudate aspirated from the wound can be utilized. In some embodiments, a superabsorbent material can be used in the absorbent layer 1212. In some embodiments, the absorbent includes a shaped form of a superabsorber layer.

A layer 1212, 1322 of absorbent material is provided above the transmission layer 1311. The absorbent material, which comprise a foam or non-woven natural or synthetic material, and which may optionally comprise a super-absorbent material, forms a reservoir for fluid, particularly liquid, removed from the wound site. In some embodiments, the layer 10 may also aid in drawing fluids towards the backing layer 1213, 1313.

The material of the absorbent layer 1212, 1322 may also prevent liquid collected in the wound dressing from flowing freely within the dressing, and preferably acts so as to contain any liquid collected within the dressing. The absorbent layer 1212, 1322 also helps distribute fluid throughout the layer via a wicking action so that fluid is drawn from the wound site and stored throughout the absorbent layer. This helps prevent agglomeration in areas of the absorbent layer. The capacity of the absorbent material must be sufficient to manage the exudates flow rate of a wound when negative pressure is applied. Since in use the absorbent layer experiences negative pressures the material of the absorbent layer is chosen to absorb liquid under such circumstances. A number of materials exist that are able to absorb liquid when under negative pressure, for example superabsorber material. The absorbent layer 1212, 1322 may typically be manufactured from ALLEVYN™ foam, Freudenberg 114-224-4 or Chem-Posite™11C-450. In some embodiments, the absorbent layer 1212, 1322 may comprise a composite comprising superabsorbent powder, fibrous material such as cellulose, and bonding fibers. In a preferred embodiment, the composite is an airlaid, thermally-bonded composite.

In some embodiments, the absorbent layer 1212, 1322 is a layer of non-woven cellulose fibers having super-absorbent material in the form of dry particles dispersed throughout. Use of the cellulose fibers introduces fast wicking elements which help quickly and evenly distribute liquid taken up by the dressing. The juxtaposition of multiple strand-like fibers leads to strong capillary action in the fibrous pad which helps distribute liquid. In this way, the super-absorbent material is efficiently supplied with liquid. The wicking action also assists in bringing liquid into contact with the upper cover layer to aid increase transpiration rates of the dressing.

The wound dressing layers of the electronics area and the absorbent layer can be covered by one continuous cover layer or backing layer 1213. As used herein, the terms cover layer and/or backing layer can be used interchangeably to refer to the layer of material in the dressing configured to cover the underlying dressing layers and seal to the wound contact layer and/or the skin surrounding the wound. In some embodiments, the cover layer can include a moisture vapor permeable material that prevents liquid exudate removed from the wound and other liquids from passing through, while allowing gases through.

The backing layer 1213, 1313 is preferably gas impermeable, but moisture vapor permeable, and can extend across the width of the wound dressing 100. The backing layer 1213, 1313, which may for example be a polyurethane film (for example, Elastollan SP9109) having a pressure sensitive adhesive on one side, is impermeable to gas and this layer thus operates to cover the wound and to seal a wound cavity over which the wound dressing is placed. In this way, an effective chamber is made between the backing layer 1213, 1313 and a wound site where a negative pressure can be established. The backing layer 1213, 1313 is preferably sealed to the wound contact layer 1310 in a border region around the circumference of the dressing, ensuring that no air is drawn in through the border area, for example via adhesive or welding techniques. The backing layer 1213, 1313 protects the wound from external bacterial contamination (bacterial barrier) and allows liquid from wound exudates to be transferred through the layer and evaporated from the film outer surface. The backing layer 1213, 1313 preferably comprises two layers; a polyurethane film and an adhesive pattern spread onto the film. The polyurethane film is preferably moisture vapor permeable and may be manufactured from a material that has an increased water transmission rate when wet. In some embodiments, the moisture vapor permeability of the backing layer increases when the backing layer becomes wet. The moisture vapor permeability of the wet backing layer may be up to about ten times more than the moisture vapor permeability of the dry backing layer.

The electronics area 1261 can include a source of negative pressure (such as a pump) and some or all other components of the TNP system, such as power source(s), sensor(s), connector(s), user interface component(s) (such as button(s), switch(es), speaker(s), screen(s), etc.) and the like, that can be integral with the wound dressing. For example, the electronics area 1261 can include a button or switch 1211 as shown in FIGS. 3A-3B. The button or switch 1211 can be used for operating the pump (e.g., turning the pump on/off).

The absorbent area 1260 can include an absorbent material 1212 and can be positioned over the wound site. The electronics area 1261 can be positioned away from the wound site, such as by being located off to the side from the absorbent area 1260. The electronics area 1261 can be positioned adjacent to and in fluid communication with the absorbent area 1260 as shown in FIGS. 3A-3B. In some embodiments, each of the electronics area 1261 and absorbent area 1260 may be rectangular in shape and positioned adjacent to one another.

In some embodiments, additional layers of dressing material can be included in the electronics area 1261, the absorbent area 1260, or both areas. In some embodiments, the dressing can comprise one or more spacer layers and/or one or more absorbent layer positioned above the wound contact layer 1310 and below the cover layer 1213, 1313 of the dressing.

FIG. 3C is a side cross-sectional view of a wound dressing system 1300, according to some embodiments. As shown in FIG. 3C, the wound dressing system 1300 can include a wound dressing 1302 with one or more embedded (also referred to as integrated) electronic components 1350. The wound dressing 1302 can include an absorbent area 1360 and an electronics area 1361. In some embodiments, the electronic components 1350 can be positioned within the wound dressing 1302 in the electronics area 1361, although it should be appreciated that the electronic components 1350 can be integrated with the wound dressing 1302 in any suitable arrangement (e.g., disposed on and/or positioned within the wound dressing 1302, among other arrangements). The electronic components 1350 can optionally include a pump 1304, a power source, a controller, and/or an electronics package, although any suitable electronic component is appreciated. The pump 1304 can be in fluidic communication with one or more regions of the wound dressing 1302, such as, for example, the absorbent area 1360 of the dressing. The absorbent area 1360 and the electronics area 1361 of the wound dressing 1302 can have any suitable arrangement. For example, FIG. 3C illustrates an embodiment of the wound dressing 1302 in which the electronics area 1361 is offset from the absorbent area 1360.

As shown in FIG. 3C, the wound dressing 1302 can include a wound contact layer 1310 and a moisture vapor permeable film or cover layer 1313 that encloses one or both of the absorbent area 1360 and the electronics area 1361. The cover layer 1313 can seal at the perimeter of the cover layer 1319 to the wound contact layer 1310 at the perimeter of the wound contact layer. In some embodiments, the dressing can optionally include an upper spacer layer or first spacer layer 1317 that includes a continuous layer of spacer material positioned below the cover layer 1313 and above the layers of the absorbent area and the layers of the electronics area. The continuous layer of spacer material or upper spacer layer 1317 can enable an air pathway between the two areas of the dressing.

The absorbent area 1360 of the dressing can include a second spacer layer 1311 or lower spacer layer and an absorbent layer 1322 positioned above the wound contact layer 1310. The second spacer layer 1311 can allow for an open air path over the wound site. The absorbent layer 1322 can include a super absorber positioned in the absorbent area 1360 of the dressing. The absorbent layer 1322 can retain wound fluid within thereby preventing fluid passage of wound exudates into the electronics area 1361 of the dressing. The wound fluids can flow through the wound contact layer 1310, to the lower spacer layer 1311, and into the absorbent layer 1322. The wound fluids are then spread throughout the absorbent layer 1322 and retained in the absorbent layer 1322 as shown by the directional arrows for wound fluids in FIG. 3C.

The electronics area 1361 of the dressing can include a plurality of layers of spacer material 1351. In some embodiments, the electronic components 1350 can be embedded within the plurality of layers of spacer material 1351. The layers of spacer material can optionally have recesses or cut outs to embed the electronic components within whilst providing structure to prevent collapse. As described above, the electronic components 1350 can optionally include a pump, a power source, a controller, and/or an electronics package, although any suitable electronic component is appreciated. A partition 1362 can optionally be positioned between the absorbent area 1360 and the electronics area 1361. The partition 1362 can separate the absorbent layer 1322 and lower air flow spacer layer 1311 from the electronic housing segment of the dressing in the electronic area. The partition 1362 can prevent wound fluid (e.g., wound exudate) from entering the electronic housing section of the dressing. In some embodiments, the partition can be a non-porous dam or other structure. The non-porous dam 1362 can include a cyanoacrylate adhesive bead or a strip of silicone. The air pathway through the dressing is shown in FIG. 3C by directional arrows. The air flows through the wound contact layer 1310, the lower spacer layer 1311, and the absorbent layer 1322 and into the first spacer layer 1317. The air can travel horizontally through the first spacer layer 1317 over and around the partition 1362 into the electronics area of the dressing.

As shown in FIG. 3C, the wound dressing system 1300 can include a fluid ingress inhibition component 1510 in fluid communication with a pump 1304. The component 1510 can allow gas (e.g., air) but inhibit liquid (e.g., wound exudate) from passing through. In some embodiments, the wound dressing layers and the component 1510 can be used with or without the optional partition 1362. The component 1510 can provide a plurality of flow paths between an interior of the wound dressing 1302 and the pump 1304 so that occlusion (e.g., from wound exudate) of the pump 1304 is inhibited. Advantageously, should any of the plurality of flow paths become occluded, one or more of the other flow paths of the plurality will be able to maintain an uninterrupted flow path between the wound dressing 1302 and the pump 1304. Such flow path redundancy can advantageously make operation of wound dressing systems 1300 more stable and reliable. In this way, the component 1510 can allow a more stable target pressure to be delivered to a wound site by ensuring that there is an open flow path between the wound dressing 1302 and the pump 1304 and by inhibiting occlusions that would otherwise cause the target pressure to be more varied. In some embodiments, the surface area of the component 1510 can advantageously increase the contact area between the pump 1304 and the wound dressing 1302, thereby providing more flow paths into the inlet of the pump 1304 for the same sized inlet. In some embodiments, the wound dressing system 1300 can include two or more components 1510. For example, in some embodiments, the wound dressing system 1300 can include between two and ten or more components 1510. The exact number used may depend on a number of factors, including the size of the wound site and the wound exudate discharge rate, in addition to the space constraints of the wound dressing, as well as other factors.

In some embodiments, the component 1510 can be made of a hydrophobic material that repels wound exudate, thereby inhibiting the ingress of fluid into the component 1510 and ultimately the pump 1304. In some embodiments, component 1510 can be a hydrophobic coated material. In some embodiments, the component 1510 can be made of a porous material. The pores can be small enough to inhibit the ingress of fluid through the component 1510 due to capillary action (i.e., from surface tension of the wound exudate against the component 1510) and the pressure differential between the environment and the wound dressing, but large enough to permit the passage of air. For example, in some embodiments, the component 1510 can be made of a material that has a pore size in the range of approximately 20 microns to approximately 100 microns. For example, in some embodiments, the material of the component 1510 can have a pore size of approximately 30 microns. In some embodiments, the material of the component 1510 can have a pore size of approximately 10 microns. However, it will be understood that any suitable pore size is appreciated. In some embodiments, the component can be a foam or a foam-like material. The hydrophobic nature of the material of the component 1510 and/or its pore size can function to inhibit the flow of wound exudate from the wound dressing 1302 to the pump 1304. The component 1510 thereby inhibits the pump 1304 in the wound dressing system 1300 from discharging wound exudate from the wound dressing 1302.

As described above, the material of the component 1510 can be porous. In some embodiments, the plurality of flow paths through the component 1510 can be defined by a series of sequentially connected pores formed in the material of the component 1510, beginning with pore(s) in fluid communication with an interior of the wound dressing 1302 and positioned on the exterior of the component 1510 and ending with pore(s) in fluid communication with the pump 1304 and positioned on the interior of the component 1510. Pores advantageously provide flow path redundancy because of their lattice arrangement and interconnected structure. The plurality of flow paths through the component 1510 that connect the first pore(s) in fluid communication with an interior of the wound dressing 1302 and the last pore(s) in fluid communication with the pump 1304 can be straight and/or tortuous. A group of open pores can effectively create one or more larger flow channels through the component 1510 that can sizably adjust as one or more occlusions materialize inside and/or outside the component 1510. In some embodiments, one or more pores can define one or more overlapping flow paths. For example, if one or more adjacent and/or neighboring pores of an open pore become occluded by wound exudate, the open pore can maintain an open path from the wound dressing 1302 to the pump 1304 by helping to redefine one or more flow paths around the one or more occluded pores. It will be appreciated that the plurality of flow paths through the component can be formed with any suitable structure. For example, in addition to or in lieu of pores, the plurality of flow paths can be formed by one or more channels extending through the component 1510.

In some embodiments, the component 1510 can be a porous polymer component. The porous polymer component can be machined and/or molded (e.g., injection molded) into any suitable shape. For example, FIGS. 4A-4C illustrate three differently shaped porous polymer components 1510 in fluid communication with a pump 1304. FIG. 4A illustrates a crescent-shaped component 1510. FIG. 4B illustrates a thimble-shaped component 1510 with a cylindrical body and rounded terminal end. FIG. 4C illustrates two thimble-shaped components 1510 with cylindrical bodies and flat terminal ends. Each of the components 1510 can allow gas (e.g., air) to pass from various points in the wound dressing (not shown) into the pump 1304 through one or more of a plurality of flow paths. The porous polymer component can be formed from POREX®, PORVAIR®, or any other suitable hydrophobic material, such as, for example, polyethylene and/or polypropylene, among others. In some embodiments, the porous polymer component can be formed from PORVAIR Vyon® porous polymer. As described above, the material of the component 1510 can be made of a material that has a pore size in the range of approximately 5 microns to approximately 100 microns (e.g., 5 microns, 100 microns). For example, in some embodiments, the material of the component 1510 can have a pore size of approximately 30 microns (e.g., 30 microns). In some embodiments, the material of the component 1510 can have a pore size of approximately 10 microns (e.g., 10 microns). However, it will be understood that any suitable pore size is appreciated.

The components 1510 shown in FIGS. 4A-4C are shown directly or indirectly coupled to an inlet 1304 a of the pump 1304. For example, FIG. 4A illustrates a component 1510 directly coupled to the pump inlet 1304 a and FIGS. 4B and 4C illustrate components 1510 indirectly coupled to the pump inlet 1304 a via an intermediate tubular member 1512. FIG. 4C also illustrates a Y-shaped splitter 1514 that connects the two components 1510 to the intermediate tubular member 1512. In some embodiments, the intermediate tubular member 1512 and the Y-shaped splitter 1514 in FIG. 4C can be a unitary piece. The internal diameter of the intermediate tubular member 1512 and the Y-shaped splitter 1514 can be in the range of approximately 1 mm to approximately 3 mm, such as for example, 2 mm. Of course, it will be understood that any suitable arrangement and structure is appreciated.

Although not shown in FIGS. 4A-4C, a non-return valve and/or an exhaust system can be coupled to the pump outlet 1304 b. Additional disclosure relating to exhaust systems and non-return valves can be found in International Application No. PCT/EP2017/055225, filed Mar. 6, 2017, titled “WOUND TREATMENT APPARATUSES AND METHODS WITH NEGATIVE PRESSURE SOURCE INTEGRATED INTO WOUND DRESSING,” which is hereby incorporated by reference in its entirety, the disclosure of which is considered to be part of the present application. Advantageously, the component 1510 can inhibit wound exudate from being drawn from the wound site through the pump and into the non-return valve and/or exhaust system.

FIGS. 5A-5C illustrate cross-sectional views of the corresponding components 1510 shown in FIGS. 4A-4C, respectively. For example, FIG. 5A illustrates the component 1510 of FIG. 4A having a port 1511 that receives a portion of the pump inlet 1304 a. FIGS. 5B and 5C similarly illustrate components 1510 having ports 1511. In some embodiments, the component 1510 can receive a portion of and/or be bonded to the member to which it connects (e.g., a pump inlet). For example, in some embodiments, the component 1510 in FIG. 5A can be bonded (e.g., glued or heat welded) to the pump inlet 1304 a. In some embodiments, the component 1510 in FIG. 5A can freely slide over the pump inlet 1304 a. One or more surrounding features of the wound dressing system 1300 can help keep the component in place (e.g., compression between the cover layer 1313 and the wound contact layer 1310 shown in FIG. 3C).

FIGS. 6A and 6B illustrate a fluid ingress inhibition system similar to the system of FIG. 5C sitting on top of a wound dressing padding or other wound dressing layer. FIG. 6A illustrates two components 1510 sitting on top of a layer of the dressing with the cover layer 1313 removed. FIG. 6B shows FIG. 6A with the cover layer 1313 or other dressing layer drawn down onto the various internal components, including the two components 1510.

In some embodiments, the component 1510 does not reduce the pump flow rate by more than 50 mL/min. For example, in some embodiments, the component 1510 can reduce the pump flow rate in the range of 15 mL/min to 35 mL/min (e.g., from 21 mL/min to 31 mL/min). In some embodiments, the component 1510 does not reduce the free performance of the pump by more than 10%. For example, in some embodiments, the component 1510 can reduce the free performance of the pump in the range of 4% to 6%.

In some embodiments, the component 1510 can be a micro porous membrane attached to a pump inlet. In some embodiments, the membrane can be formed into the shape of a pouch to fit over and attach to the pump inlet. A 3d spacer (e.g., fabric) can be disposed in the pouch to inhibit the membrane from collapsing. In some embodiments, the pouch can be elongate in form, but it will be appreciated that the pouch can take on any suitable form. The membrane can be hydrophobic to repel fluid (e.g., wound exudate) and have a porosity that inhibits fluid ingress into the pump inlet due to capillary action. For example, in some embodiments, the micro porous membrane can be made of Versapore having a 0.2 μm pore size (Pall).

In some embodiments, the component 1510 can be one or more lengths of fine bore tubing with a plurality of holes disposed along their lengths. The one or more lengths of fine bore tubing can form one or more loops between a pump inlet and a wound dressing. As another example, the one or more lengths of fine bore tubing can extend from the pump inlet to one or more different points in the wound dressing, similar to the way in which the two components 1510 in FIGS. 6A and 6B are positioned at two different points in the wound dressing. The size of the bore in the tubing can have an internal diameter such that the tubing resists collapse under reduce pressure.

In some embodiments, the component 1510 is designed so that a significant pressure drop is avoided by its use. In this way, the component 1510 prevents the pump 1304 from having to work harder and consume more power from any added resistance it may add to the flow path from the wound dressing to the environment through the pump 1304.

FIGS. 7A and 7B illustrate embodiments of an electronics unit 1700 including a pump 1704 and a component 1710 directly coupled to the pump inlet 1704 a. FIG. 7A illustrates the top view of the electronics unit. FIG. 7B illustrates a bottom or wound facing surface of the electronics unit. The electronics unit 1700 can include a pump and other electronic component such as power source(s), sensor(s), connector(s), circuit board(s), user interface component(s) (such as button(s), switch(es), speaker(s), screen(s), etc.) and the like. In some embodiments, the electronics unit of FIGS. 7A-7B can be embedded into the electronics area 1361 of the wound dressing as one unit.

In some embodiments, the component 1710 can be pushed onto the pump inlet. This can be a friction fit. The port of the component 1710 that receives a portion of the pump inlet can be sized and shaped to be a complementary fit around the pump inlet. In some embodiments, the component 1710 can be bonded onto the pump inlet using a silicone sealant or any other sealant or sealing technique. In some embodiments, the electronics unit can be embedded within layers of the dressing in the electronics area 1361. In some embodiments, the layers of the dressing in the electronics area 1361 can include cutouts or recesses into which the electronics unit 1700 can be placed.

FIG. 8 illustrates the wound dressing layers for embedding or integrating an electronics unit. As illustrated in FIG. 8, the dressing can include a wound contact layer 1310 for placing in contact with the wound. Lower spacer layers 1311 and 1311′ are provided above the wound contact layer 1310. In some embodiments, the spacer layer 1311 can be a separate layer from spacer layer 1311′ as shown in FIG. 8. In other embodiments, the lower spacer layers 1311 and/or 1311′ can be a continuous layer of spacer material that is below both the electronics area and the absorbent area. The lower spacer layers 1311 and 1311′ can assist in distributing pressure evenly to the wound surface and/or wicking fluid away from the wound. An absorbent layer 1322 can be positioned above the lower spacer layer 1311 and/or 1311′. A dressing layer 1351 can include cutouts or recesses 1328 for embedding the electronic components 1350 within the layer 1351. In some embodiments, the layer 1351 can be an absorbent material. In some embodiments, the dressing layer 1351 and absorbent layer 1322 can be one continuous piece of absorbent material. Alternatively, in some embodiments, the layer 1351 can be a spacer layer or transmission material. In some embodiments, the cutouts or recesses 1328 can be sized and shaped to embed a pump 1327, power source 1326, and/or other electronic components of the electronics unit. In some embodiments, the pump 1327, power source 1326, and/or other electronic components can be incorporated into the cutouts or recesses 1328 as individual components or as an electronic assembly as shown in FIGS. 7A-7B. An upper layer 1317 optionally can be provided above the absorbent layer 1322, layer 1351, and/or electronic components 1350. A cover layer or backing layer 1313 can be positioned over the upper spacer layer. In some embodiments, when the upper layer 1317 is not used, the cover layer or backing layer 1313 can be provided above the absorbent layer 1322, layer 1351, and/or electronic components 1350. The backing layer 1313 can form a seal to the wound contact layer 1310 at a perimeter region enclosing the spacer layers 1311, 1311′, and 1317, the absorbent layer 1322, layer 1351, and electronic components 1350. In some embodiments, the backing layer 1313 can be a flexible sheet of material that forms and molds around the dressing components when they are applied to the wound. In other embodiments, the backing layer 1313 can be a material that is preformed or premolded to fit around the dressing components as shown in FIG. 8.

The component 1710 can be provided on the inlet of the pump 1327. In some embodiments, the hydrophobicity of the component 1710 can keep the inlet to the pump free of exudate. In some embodiments, the component 1710 can be in contact with and/or in fluid communication with superabsorbent and/or absorbent material. In this configuration, the component 1710 can prevent liquid from being pulled through to the inlet of the pump when negative pressure is applied. The component 1710 can be made of a material with a pore size larger than the pore size of traditional hydrophobic filters and liquid could get through if the material of the component were by itself in contact with water. However, the hydrophobicity of the hydrophobic component 1710 with a pore size as described herein can be in contact with the superabsorber and/or absorbent material and can prevent exudate from being pulled through the inlet of the pump when negative pressure is applied.

FIG. 9A-9B illustrates an embodiment of a component 1710 with a port 1715 for coupling to the pump inlet. The port 1715, similar to port 1511 of FIGS. 5A-5C, is shaped to receive a portion of the pump inlet 1304 a. In some embodiments, the shape of the pump inlet 1304 a can be tubular or cylindrical as shown in the cross-section of the pump inlet 1304 a in FIG. 5A. In some embodiments, the component 1710 can receive a portion of and/or be bonded to the member to which it connects (e.g., a pump inlet). For example, in some embodiments, the component 1710 can be bonded (e.g., glued or heat welded) to the pump inlet 1304 a. In some embodiments, the component 1710 can freely slide over the pump inlet 1304 a. One or more surrounding features of the wound dressing system can help keep the component in place (e.g., compression between the cover layer and the wound contact layer).

In some embodiments, the component 1710 can have a 3-dimensional shape and circumferentially surrounds the pump inlet. The 3-dimensional shaped component 1710 can have a width, height, and/or length dimension that is greater than the width, height, and/or length of the pump inlet 1304 a. In some embodiments, the component 1710 can be a cuboid or generally cuboid shape as shown in FIGS. 9A and 9B. For example, the component 1710 may have a flat pump-facing surface through which the port 1715 extends, with one or more beveled edges and/or corners. In some embodiments, the 3-dimensional component can circumferentially surround the pump inlet when the pump inlet is inserted into the port 1715 of the component 1710. By circumferentially surrounding the pump inlet, the 3-dimensional component can provide a surface area larger than the surface area available at the pump inlet 1304 a. The larger surface area can provide a plurality of flow paths within the component 1710. This can allow air to be drawn through a portion of the component 1710 even when another portion of the component 1710 is surrounded by fluid or otherwise blocked.

All of the features disclosed in this specification (including any accompanying exhibits, claims, abstract and drawings), and/or all of the steps of any method or process so disclosed, may be combined in any combination, except combinations where at least some of such features and/or steps are mutually exclusive. The disclosure is not restricted to the details of any foregoing embodiments. The disclosure extends to any novel one, or any novel combination, of the features disclosed in this specification (including any accompanying claims, abstract and drawings), or to any novel one, or any novel combination, of the steps of any method or process so disclosed.

Various modifications to the implementations described in this disclosure may be readily apparent to those skilled in the art, and the generic principles defined herein may be applied to other implementations without departing from the spirit or scope of this disclosure. Thus, the disclosure is not intended to be limited to the implementations shown herein, but is to be accorded the widest scope consistent with the principles and features disclosed herein. Certain embodiments of the disclosure are encompassed in the claim set listed below or presented in the future. 

1.-25. (canceled)
 26. A wound dressing apparatus comprising: a wound dressing configured to be positioned over a wound site; a negative pressure source disposed on or positioned within the wound dressing, the negative pressure source comprising an inlet and an outlet and being operable to apply negative pressure to the wound site; and a porous polymer component fitted to the inlet of the negative pressure source and in fluid communication with the inlet, the porous polymer component comprising a three-dimensional body defining a plurality of flow paths between an interior of the wound dressing and the inlet such that occlusion of the inlet is inhibited.
 27. The wound dressing apparatus of claim 26, wherein at least a portion of the plurality of flow paths is configured to directly contact a portion of the inlet.
 28. The wound dressing apparatus of claim 26, wherein the porous polymer component comprises a port configured to receive at least a portion of the inlet.
 29. The wound dressing apparatus of claim 26, wherein the component comprises a hydrophobic material configured to repel wound exudate.
 30. The wound dressing apparatus of claim 26, wherein the component comprises a material having a pore size configured to resist ingress of wound exudate due to capillary action.
 31. The wound dressing apparatus of claim 26, wherein the porous polymer molded component is hydrophobic and has a pore size in the range of approximately 20 microns to approximately 40 microns.
 32. The wound dressing apparatus of claim 31, wherein the pore size is approximately 30 microns.
 33. The wound dressing apparatus of claim 26, wherein the porous polymer molded component is hydrophobic and has a pore size in the range of approximately 5 microns to approximately 40 microns.
 34. The wound dressing apparatus of claim 26, wherein the porous polymer molded component provides an increased contact area to the interior of the wound dressing.
 35. The wound dressing apparatus of claim 26, wherein the porous polymer component is one of crescent-shaped, thimble-shaped, or cuboid or generally cuboid shaped.
 36. The wound dressing apparatus of claim 26, wherein the porous polymer component comprises curved or beveled corners and/or edges.
 37. The wound dressing apparatus of claim 26, wherein the porous polymer component comprises a flat surface configured to face the negative pressure source.
 38. The wound dressing apparatus of claim 26, wherein the porous polymer component circumferentially surrounds the inlet.
 39. The wound dressing apparatus of claim 26, wherein the porous polymer component has a width, height, and/or length dimension that is greater than the width, height, and/or length of the inlet.
 40. The wound dressing apparatus of claim 26, the porous polymer component is configured to be pushed onto the inlet.
 41. The wound dressing apparatus of claim 26, wherein the wound dressing comprises a wound contact layer and a moisture vapor permeable film or a cover layer positioned above the contact layer.
 42. The wound dressing apparatus of claim 26, wherein the wound dressing comprises a wound contact layer, a spacer layer, an absorbent layer and a moisture vapor permeable film or a cover layer positioned above the wound contact layer, the spacer layer and the absorbent layer.
 43. The wound dressing apparatus of claim 26, wherein the porous polymer component is in fluid communication with the absorbent material and configured to inhibit flow of wound exudate from the wound site into the inlet.
 44. The wound dressing apparatus of claim 43, wherein the wound dressing further comprises a layer of porous material above the wound contact layer.
 45. The wound dressing apparatus of claim 26, wherein the porous polymer component is configured to permit gas but inhibit wound exudate from passing therethrough. 